| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45886047-45886235 | Common:1; Rare:72 | ||||
| chr19:45902584-45902957 | Common:3; Rare:120 | ||||
| chr19:45995080-45995553 | Common:3; Rare:185 | ||||
| chr19:46346829-46347160 | Common:3; Rare:116 | ||||
| chr19:46347323-46347335 | |||||
| chr19:46347421-46347539 | Rare:27 | ||||
| chr19:46413501-46413778 | Common:1; Rare:90 | ||||
| chr19:46471468-46471673 | Common:6; Rare:81 | ||||
| chr19:46600565-46600669 | Rare:29 | ||||
| chr19:46600671-46600705 | Rare:5 | ||||
| chr19:46600824-46601418 | Common:5; Rare:199; Clinvar (benign):1 | ||||
| chr19:46634218-46634509 | Common:2; Rare:48 | ||||
| chr19:46661168-46661445 | Rare:77 | ||||
| chr19:46713774-46714052 | Common:1; Rare:83 | ||||
| chr19:46714268-46714506 | Common:2; Rare:47 |